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	<title>Darrin's Day.com &#187; dclock</title>
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	<link>http://www.darrinsday.com</link>
	<description>Where one more day means everything......</description>
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		<title>Katee&#8217;s Done with Chemotherapy!!!</title>
		<link>http://www.darrinsday.com/2008/02/07/katees-done-with-chemotherapy/</link>
		<comments>http://www.darrinsday.com/2008/02/07/katees-done-with-chemotherapy/#comments</comments>
		<pubDate>Thu, 07 Feb 2008 18:46:00 +0000</pubDate>
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		<guid isPermaLink="false">http://www.darrinsday.com/2008/02/07/katees-done-with-chemotherapy/</guid>
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			<content:encoded><![CDATA[<p>Finally, Katee has completed her last chemo treatment today.  She was supposed to be done a couple of days ago, but there was a malfunction in the chemo pump that she wears at night.  It came loose and blood spilled out of the device and her chemo ports.  They could not be sure that she had received the correct dose, so she had to take another dose, and wear the device another night.  However, today was the last treatment.  Katee will go in two weeks from now to make sure her blood work is returning to normal.  She will have a PET scan in about 30 days to ensure that the cancer is fully dead.  At this time all indications are that she is cancer free and doing great!   What a huge relief.  I am so proud of her and her strength to get through all these treatments.  She is so strong and did a great job in taking a tough chemotherapy dosages.<span id="more-60"></span></p>
<p>We would like to thank everyone who participated in the fund raiser in conjunction with the Senior Center of Castle Rock.  Once again, the thoughtfulness and generosity of the Castle Rock community was more that we could ever expect.  We received enough money from the fund raiser to compensate for my moving to disability and the expenses of fighting cancer.  Thank you so much.  We are truly blessed to be surrounded by such good friends.</p>
<p>My chemo is going well.  I am sick quite a bit, but it is tolerable.  Today my hair started falling out again.  It is not as traumatic as last time, I guess you just get used to it.  I have 5 more weeks of treatment before we find out if it is working this time.  The wait is difficult, but I feel that a great weight has been lifted with the completion of Katee&#8217;s chemo.  Her successful treatment has given me hope that I will also get a positive result from my treatment. </p>
<p>Again, I want to thank all of you that keep us in your thoughts and prayers.  We deeply appreciate all that each one of you have done for our family.  To those that have given to us financially, please know that we are so grateful and use the money only toward the cost of fighting cancer.  We wish we could repay you all, but all we can do is offer our prayers and blessings upon you all.  Thank You!</p>
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		<slash:comments>4</slash:comments>
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		<title>We Have A Plan!</title>
		<link>http://www.darrinsday.com/2008/01/12/we-have-a-plan/</link>
		<comments>http://www.darrinsday.com/2008/01/12/we-have-a-plan/#comments</comments>
		<pubDate>Sat, 12 Jan 2008 16:35:46 +0000</pubDate>
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		<guid isPermaLink="false">http://www.darrinsday.com/2008/01/12/we-have-a-plan/</guid>
		<description><![CDATA[I met with my Oncologist last week, and we had a long and through discussion on my test results and options.  We have chosen a path that has not been tried before, at least as far as any of us know.  My Oncologist suggested a cocktail of chemo drugs, with an additional medication that is [...]]]></description>
			<content:encoded><![CDATA[<p>I met with my Oncologist last week, and we had a long and through discussion on my test results and options.  We have chosen a path that has not been tried before, at least as far as any of us know.  My Oncologist suggested a cocktail of chemo drugs, with an additional medication that is not used for chemo, but has been used in the past with interesting results.  It was determined that if I do not try some sort of therapy, my life would end in May 2008.  I refuse to accept that date, so after a discussion with my family, we have decided to start the following therapy.<span id="more-58"></span></p>
<p>The cocktail we will be trying is a cocktail containing Ifex, Gemzar, Taxotere and Vevaprimil.  I will be taking this cocktail through an IV for 5 days in a row the first week, then once a week for week 2 and 3.  During week 2 and 3 I will be getting many different drugs on days that I don&#8217;t have chemo, to try to reduce the side-effects of the chemo cocktail.   They will try to keep my blood marrow working, red blood cell count up and to protect my other organs that are at risk from this chemo cocktail, specifically my Liver, Bladder and Kidneys.</p>
<p> Due to this schedule, I will not be able to return to work for at least the 8 weeks of this chemotherapy.  The Doctor has suggested that with my low oxygen levels and chronic pain I already have from the two previous surgeries, I would not be able to work with the additional effects this chemo will have.  Specifically, they expect I will have weakness, increased pain, nausea, diarrhea, bleeding and mouth sores.  There is many other expected side-effects, but the largest one is a risk of coma.  I will really miss not working with my team, but I agree that I don&#8217;t think I have the strength to work and do this chemo again, especially as I am still healing from the last lung surgery.</p>
<p>I started one of the drugs, (Vevaprimil) this week, and will start the rest of the cocktail on January 21st.  What a bummer, I just last week went and got a haircut, and now it will all fall out again!  Anyway, that is the latest with our family.  We as a family, are all in agreement to try out this chemo cocktail, so that makes things easier.  Katee is doing great and only has 2 treatments left.  She is so excited to have her treatment end.</p>
<p>Thank you to all that have stepped up and helped us out.  There are too many to recognize you all individually, but you know who you are.  Thank you so very much! </p>
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		<title>Update and Tough Decisions</title>
		<link>http://www.darrinsday.com/2008/01/05/update-and-tough-decisions/</link>
		<comments>http://www.darrinsday.com/2008/01/05/update-and-tough-decisions/#comments</comments>
		<pubDate>Sat, 05 Jan 2008 17:32:18 +0000</pubDate>
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		<guid isPermaLink="false">http://www.darrinsday.com/2008/01/05/update-and-tough-decisions/</guid>
		<description><![CDATA[Hello All, I am recovering well from my last surgery.  They removed a nodule of my cancer from my right lung, and sent this live sample to Texas for testing.  The sample they removed was larger than a golf ball, but smaller than a baseball.  I am still having some problems from the surgery, as [...]]]></description>
			<content:encoded><![CDATA[<p>Hello All, I am recovering well from my last surgery.  They removed a nodule of my cancer from my right lung, and sent this live sample to Texas for testing.  The sample they removed was larger than a golf ball, but smaller than a baseball.  I am still having some problems from the surgery, as the bottom lobe on my right lung has not yet fully inflated.  I am using a breathing machine and plenty of oxygen to assist with this.  They have told me that with time the lung will fully inflate on it&#8217;s own.  I met with my pain management Doctor last week, and he changed my medications so that I am having much less pain than before.  However, I am a bit groggy from all the medications, but they assure me I will get used to it.<span id="more-57"></span></p>
<p>The results of the testing they did on the live sample of cancer was interesting.  They did not find any evidence of my primary diagnosis of Leiomyosarcoma (LMS), but rather they found two other cancers that are closely related to LMS.  The difference is that while LMS attacks smooth muscle, these other two cancers attack connective tissue and cartilage.  They have determined that the LMS has mutated on it&#8217;s own into these two new forms.  The testing they were doing is to find a chemotherapy drug that would be effective in shrinking or killing the cancer cells.  The results of this test show only one drug that might be effective, but it only shows a 20% chance of working.  The side-effects of this chemo drug are pretty severe, with a risk of coma involved.  We are meeting with my oncologist next week to discuss the options, level of chemo drugs, side-effects and whether or not it is worth doing.  If we don&#8217;t do anything, they only expect me to live to May.  However, they have been wrong on my life expectancy before, so we are not getting too worked up over this.  It will be a family decision on whether we choose to try the chemo drugs again, or stop treatment all together. </p>
<p>I have not yet been able to return to work, primarily due to pain levels from the surgery and a lack of oxygen due to the collapsed portion of my right lung.  The meeting next week with my oncologist will help us determine when I can return to work.  At this time, the majority of my Doctors suggest that I not return to work, and enjoy the time we have left.  Again, this will be a family decision we can make once they tell me I am physically able to return to work.  I really enjoy my work with the Town of Castle Rock, and miss the team.  It would be very difficult to not return to work.  I hope it does not come to that.</p>
<p>As you can see, we have many difficult decisions to make in the next week or so.  Please pray that we get solid and correct advice from the medical staff, and enough information to make educated decisions.  On a positive note, Katee only has three more chemo treatments.  She is very tired of going to these treatments and would like to quit early.  However, she will gut it out and continue to the end of the treatments as scheduled.  Her hair is staying in pretty well, but it is taking her longer to recover from each chemo treatment.  She is very tired and ready to return to her normal life.  She will start looking for a job in March, to help her save up some money for college this fall.  She is very excited to get back to college, as she misses her friends and the social aspect she has had to give up with her chemo treatments.  She is doing very well as far as winning the war on her colon cancer, and is still cancer free.  This is certainly something we celebrate!</p>
<p> We want to say &#8220;Thank you&#8221; to all who have supported us through these tough times.  We appreciate all of you!</p>
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		<title>Tough Decisions</title>
		<link>http://www.darrinsday.com/2007/12/11/tough-decisions/</link>
		<comments>http://www.darrinsday.com/2007/12/11/tough-decisions/#comments</comments>
		<pubDate>Tue, 11 Dec 2007 15:16:30 +0000</pubDate>
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		<guid isPermaLink="false">http://www.darrinsday.com/2007/12/11/tough-decisions/</guid>
		<description><![CDATA[The Doctor visit last night did not go well.  Basically, my lungs are getting full of cancer, and this has reduced my ability to intake oxegen to a level that is getting severe.  I have elected to do a surgery to remove a 22cm cancer from my left lung.  This will be kept alive, and [...]]]></description>
			<content:encoded><![CDATA[<p>The Doctor visit last night did not go well.  Basically, my lungs are getting full of cancer, and this has reduced my ability to intake oxegen to a level that is getting severe.  I have elected to do a surgery to remove a 22cm cancer from my left lung.  This will be kept alive, and tested in a facility in Texas to see if they can find a drug that would stop the growth, or even shrink the cancer.  The chances of this working are small, but the only option we have left.  If I do nothing, they suggest that I have less than 6 months to live.  We as a family are trying to decide today when to do the surgery.  They want to do it right away, but we could wait till after Christmas.  Either way, I will be 2-3 weeks in recovery from this lung surgery.  It will take a couple of weeks after the surgery to get the results on the cancer testing.  Then we need to determine if we want to take the chemo cocktail, what benefits it will provide, and how sick I will become from it.  They also want me to quickly stop working, and rest my body in anticipation of all this work.  It sure feels like we are entering the last stage of this fight.  They (my Doctors) are no longer trying to cure my cancer, only slow the progression.  My family and I are trying to decide how much further treatment we can take, versus the quality of life for these last few months.  It is tough, as my family want to spend time with me while I am feeling okay, but if we wait, the chances of extending my life are reduced.  I sure feels like we are loosing at this time.  Please pray for us.</p>
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		<slash:comments>3</slash:comments>
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		<title>PET Scan validates earlier diagnosis</title>
		<link>http://www.darrinsday.com/2007/12/10/pet-scan-validates-earlier-diagnosis/</link>
		<comments>http://www.darrinsday.com/2007/12/10/pet-scan-validates-earlier-diagnosis/#comments</comments>
		<pubDate>Mon, 10 Dec 2007 18:49:38 +0000</pubDate>
		<dc:creator>dclock</dc:creator>
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		<guid isPermaLink="false">http://www.darrinsday.com/2007/12/10/pet-scan-validates-earlier-diagnosis/</guid>
		<description><![CDATA[We did get the results of the PET scan.  It also showed significant growth of the cancers in both lungs.  It did identify a new cancer growing very rapidly on the side of my left lung.  The current line of thinking is to have a surgery to remove a portion of that new cancer, and [...]]]></description>
			<content:encoded><![CDATA[<p>We did get the results of the PET scan.  It also showed significant growth of the cancers in both lungs.  It did identify a new cancer growing very rapidly on the side of my left lung.  The current line of thinking is to have a surgery to remove a portion of that new cancer, and send it to a lab in Texas.  They are doing some cutting edge testing on cancers in the test tube, and perhaps they can find a chemo cocktail that would slow down my progression.  They have warned us not to get our hopes up, as this is really new technology and the chances of it working are low.  The results also gave us in indication of how long I have to live, given things continue to respond the same way.  They have estimated my life expectancy at 6-8 more months.  They also identified a new growth in the left side of my &#8220;rear&#8221; that appears to be cancer spreading.  I am meeting with  a surgeon later today to discuss all my options.  However, as much as I appreciate my Doctors, I simply cannot agree with all they are saying.  I feel pretty good right now, just very tired, so it is hard to believe the diagnosis.  Katee continues to do well, and has shown so much strength and humor in all this.  She will end her chemo in February 08.  We will post new information on the site as we get it.  Please let me again thank you all that have stood with us both emotionally and financially.  Thank You!</p>
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		<slash:comments>3</slash:comments>
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		<title>Katee gets a clean scan!</title>
		<link>http://www.darrinsday.com/2007/11/27/katee-gets-a-clean-scan/</link>
		<comments>http://www.darrinsday.com/2007/11/27/katee-gets-a-clean-scan/#comments</comments>
		<pubDate>Tue, 27 Nov 2007 21:59:09 +0000</pubDate>
		<dc:creator>dclock</dc:creator>
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		<guid isPermaLink="false">http://www.darrinsday.com/2007/11/27/katee-gets-a-clean-scan/</guid>
		<description><![CDATA[Katee&#8217;s PET scan came back yesterday, and the results indicate no presence of cancer!  We are pretty excited about this.  Katee is just over halfway through her chemo treatments.  She would like to quit (as anyone who has had chemo can attest to) but these good results should encourage her to finish up the series.  [...]]]></description>
			<content:encoded><![CDATA[<p>Katee&#8217;s PET scan came back yesterday, and the results indicate no presence of cancer!  We are pretty excited about this.  Katee is just over halfway through her chemo treatments.  She would like to quit (as anyone who has had chemo can attest to) but these good results should encourage her to finish up the series. </p>
<p>I have recovered from my pneumonia, and had blood-work yesterday to ensure this was true.  If the results come back and show that I really have fully recovered, then I will have a PET scan next week.  This one will help determine how much time the doctors believe I have left.  They have been wrong so many times, I will not put much faith in the results of the PET scan.</p>
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		<title>Stopping Chemo Treatments</title>
		<link>http://www.darrinsday.com/2007/11/14/stopping-chemo-treatments/</link>
		<comments>http://www.darrinsday.com/2007/11/14/stopping-chemo-treatments/#comments</comments>
		<pubDate>Wed, 14 Nov 2007 19:35:48 +0000</pubDate>
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		<guid isPermaLink="false">http://www.darrinsday.com/2007/11/14/stopping-chemo-treatments/</guid>
		<description><![CDATA[With all the test I have gone through lately in my fight with Pneumonia, I was required to have a series of CAT scans.  These scans showed that my cancer is not responding to the chemotherapy.  In fact, it showed significant growth in all cancers and many new ones.   This is obviously very disappointing.  Given [...]]]></description>
			<content:encoded><![CDATA[<p>With all the test I have gone through lately in my fight with Pneumonia, I was required to have a series of CAT scans.  These scans showed that my cancer is not responding to the chemotherapy.  In fact, it showed significant growth in all cancers and many new ones.   This is obviously very disappointing.  Given these results and after much discussion with my doctors and family, we have elected to stop any further chemotherapy.  There does not seem to be any treatment available at this time that would help.  I will continue to take IV antibiotics for a week, and that should stop the Pneumonia.  After that, I will be simply recovering from the chemo.  Once my lungs have fully recovered from the pneumonia, I will have a PET scan that will help my oncologist to determine about how much time I have left.  Please keep us in your prayers.  We will have many big decisions to make once we have an estimate of how long I have to live.</p>
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		<slash:comments>4</slash:comments>
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		<title>Thank you for the comments!</title>
		<link>http://www.darrinsday.com/2007/11/01/thank-you-for-the-comments/</link>
		<comments>http://www.darrinsday.com/2007/11/01/thank-you-for-the-comments/#comments</comments>
		<pubDate>Fri, 02 Nov 2007 06:16:10 +0000</pubDate>
		<dc:creator>dclock</dc:creator>
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		<guid isPermaLink="false">http://www.darrinsday.com/2007/11/01/thank-you-for-the-comments/</guid>
		<description><![CDATA[We would like to thank each and every one of you that take the time to leave a comment for us on the web site.  We are so encouraged by your thoughts and kind words.  I must admit that I don&#8217;t know how to respond to the comments (and I mean I technically don&#8217;t know!) [...]]]></description>
			<content:encoded><![CDATA[<p>We would like to thank each and every one of you that take the time to leave a comment for us on the web site.  We are so encouraged by your thoughts and kind words.  I must admit that I don&#8217;t know how to respond to the comments (and I mean I technically don&#8217;t know!) but we do read them and post them for others to read.  This is the only way I know how to respond to you all.  Thank you so much.  Back to chemo tomorrow, so I will not be on the site for a few days while I recover.</p>
<p> Darrin</p>
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		<title>Back from the Hospital</title>
		<link>http://www.darrinsday.com/2007/10/30/back-from-the-hospital/</link>
		<comments>http://www.darrinsday.com/2007/10/30/back-from-the-hospital/#comments</comments>
		<pubDate>Tue, 30 Oct 2007 20:10:20 +0000</pubDate>
		<dc:creator>dclock</dc:creator>
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		<guid isPermaLink="false">http://www.darrinsday.com/2007/10/30/back-from-the-hospital/</guid>
		<description><![CDATA[I was admitted very early Sunday morning to SkyRidge Hospital, as I was unable to stop throwing up blood.  This is not an uncommon occurrence for people on chemo, but this one was a bit more than we have experienced in the past.  Anyway, it is Tuesday afternoon, and I am so glad to be [...]]]></description>
			<content:encoded><![CDATA[<p>I was admitted very early Sunday morning to SkyRidge Hospital, as I was unable to stop throwing up blood.  This is not an uncommon occurrence for people on chemo, but this one was a bit more than we have experienced in the past.  Anyway, it is Tuesday afternoon, and I am so glad to be home.  I am feeling much better, and a change in some medications should help from this happening again.  Katee is back in chemo this week.  She has completed her Iron infusions, so she only needs to go to the infusion center for chemo every two weeks.  We are still hopeful that Katee can stop all further treatment and have a clean bill of health near the beginning of March 2008.  I know she is ready to get back to her life and school!  <span id="more-47"></span>I will have a PET scan in a couple of weeks that will help us determine if the chemo is working on my cancer.  We are praying that it has really been impacted with this chemo treatment.  The plan is to continue the chemo indefinitely, or at least as long as I show positive results.  Perhaps in 6 to 8 months we can consider further surgeries, to get the larger cancer nodes removed.  While the medical community would be happy if I continue to show positive results, I would like to take it a step further and have an opportunity to stop chemo treatment for a while without risking a long-term prognosis.  However, I will not complain as I am doing better than most anyone gave us a hope to.  Thank you to all who continue to support us.  Your kind words, thoughts and prayers are encouraging, probably more than you will ever know.</p>
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		<title>What is it like to have cancer, from a Mothers perspective (Part 1)</title>
		<link>http://www.darrinsday.com/2007/10/30/what-is-it-like-to-have-cancer-from-a-mothers-perspective-part-1/</link>
		<comments>http://www.darrinsday.com/2007/10/30/what-is-it-like-to-have-cancer-from-a-mothers-perspective-part-1/#comments</comments>
		<pubDate>Tue, 30 Oct 2007 19:53:23 +0000</pubDate>
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		<guid isPermaLink="false">http://www.darrinsday.com/2007/10/30/what-is-it-like-to-have-cancer-from-a-mothers-perspective-part-1/</guid>
		<description><![CDATA[To Darrin &#38; Katee: I read your article regarding what it is like to have cancer from your perspective.  It touched my heart.  I wanted to tell you what it is like from my perspective.  As your Mother, my heart feels like it is broken and will never heal.  You are my firstborn and are [...]]]></description>
			<content:encoded><![CDATA[<p class="EC_MsoNormal"><font face="Calibri">To Darrin &amp; Katee:</font></p>
<p class="EC_MsoNormal"><font face="Calibri">I read your article regarding what it is like to have cancer from your perspective.  It touched my heart.  </font><font face="Calibri">I wanted to tell you what it is like from my perspective.  As your Mother, my heart feels like it is broken and will never heal.  You are my firstborn and are irreplaceable.  </font><font face="Calibri">There is not a day, hour or minute that goes by that I don’t think about you and Katee and it causes tremendous sadness in my soul.  At night I wake up thinking about you and praying for you.  Wondering where is God, why doesn’t He heal you.  Often I can sense in my spirit when you or Katee are having a bad day or night and I just have to call to hear your voices.  I want to hear all the details, good or bad.  When you or Katee are sad or sick, I am sad as well.   To me, cancer is a totally consuming disease for all of those involved in one way or another.  </font><font face="Calibri">When I think that it could be possible that I would lose you, son, I am sad, tearful and angry.  I enjoy so much your personality, your great sense of humor and your extraordinary intelligence.  I am really not ready to let God have you to Himself!  </font><font face="Calibri">I have watched you suffer so much with this cancer and I have grieved with you over all you have lost.  I have tried to be there for you during your surgeries, your chemo and also times when you feel a little better and we can laugh and forget for just a few minutes about cancer.  As a Mother, I want to be able to “fix” it, but I can’t and it is so frustrating for me.  </font><font face="Calibri">Last month when I came to sit with Katee during her chemo time, it generated such mixed feelings.  I was proud of her for her courage, sorrowful for her for her pain and all she has had to deal with during her diagnosis.  I could tell she brought joy and encouragement to the others on the chemo unit and yet she herself was hurting.  I am glad for her friends who are a source of encouragement to her and for her sister Ami, who devotes all the time and love she can to Katee.  </font><font face="Calibri">I have watched your family suffer with you, cry with you and laugh with you.  You have been especially blessed with a wonderful wife, Kim who has in spite of everything, held it all together for us.  For her I am extremely grateful.  </font><font face="Calibri">How has cancer changed me?  I am not sure.  It has consumed my life and my thoughts.  It has definitely caused me to pray more, to be less concerned with little petty things in my life and to value each of my family members more.  We hug more, we tell each other we love them more, because we know the value of each day! </font></p>
<p class="EC_MsoNormal"><font face="Calibri">I love you son,</font></p>
<p class="EC_MsoNormal"><font face="Calibri">Mom</font></p>
<p class="EC_MsoNormal"><font face="Calibri">  </font></p>
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